Quality Control Analyst (2nd shift)

Novartis•Millburn, NJ

2d•Onsite

About The Position

Novartis is hiring a Quality Control Analyst for an on-site role in Millburn, New Jersey. The analyst performs chemical and microbiological testing of products, raw materials, and packaging components while supporting the readiness and day-to-day execution of Quality Control operations. The work involves analytical instrumentation, environmental monitoring, sterility testing, investigations, and documentation, with a focus on quality, safety, and regulatory compliance. This second-shift role follows a 4x10 schedule, with expected hours of 3:00 p.m. to 1:30 a.m. on either Sunday–Wednesday or Wednesday–Sunday. Schedule adjustments may be needed based on business needs. Novartis does not offer relocation support for this role. The expected annual salary range is $85,400 to $158,600. Final compensation depends on factors including relevant skills and experience. Compensation includes a performance-based cash incentive and, depending on role level, potential eligibility for annual equity awards. Eligible U.S.-based employees receive health, life, and disability benefits, a 401(k) with company contribution and match, other benefits, and paid time off including vacation, personal days, holidays, and other leaves.

Requirements

Bachelor's degree in Chemistry, Microbiology, or another relevant scientific discipline.
At least two years of experience working in a GMP or aseptic environment.
Hands-on experience with physicochemical techniques and analytical instrumentation, including HPLC, GC, and iTLC.
Knowledge of GMP regulations and FDA guidance applicable to Quality Control testing.
Understanding of aseptic principles and techniques, including environmental monitoring and sterility testing.
Ability to interpret analytical data and translate results into clear, accurate technical documentation.

Nice To Haves

Experience supporting deviation investigations, corrective and preventive actions, change controls, or qualification and validation activities.
Experience with Quality Control testing and documentation in an RLT or radiopharmaceutical environment.

Responsibilities

Perform chemical and microbiological testing of raw materials, finished products, and packaging components.
Execute environmental monitoring and sterility testing in compliance with GMP requirements.
Prepare, operate, clean, and maintain Quality Control equipment, reagents, materials, and testing areas.
Manage samples, document testing activities, report results, and escalate deviations or nonconformances.
Support investigations, corrective and preventive actions, change controls, and related procedure and form revisions.
Participate in equipment, method, and process qualification and validation activities as assigned.
Prepare accurate analytical records and support internal and external audits and regulatory inspections.